Clinical Trial Administrator

Your new role

As Clinical Trial Administrator, you will be the operational backbone of our local study team – ensuring trials are set up, executed and closed out with precision, quality and full regulatory compliance. You will work across every phase of the trial lifecycle, collaborating with sites, vendors and cross‑functional colleagues to keep our clinical activities running smoothly.

Day‑to‑day responsibilities

• Providing administrative, logistical and operational support across all phases of clinical trials, from start‑up through close‑out
• Setting up and maintaining the eTMF, Investigator Site File (ISF) and Novo Nordisk Investigator Portal, ensuring document quality and timely archiving
• Supporting study start‑up, including document submission to Regulatory Authorities and Ethics Committees, ‘Green Light’ checks and drug release documentation
• Coordinating clinical supply activities and liaising with Vendor ...